| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:47778400-47778747 | Common:2; Rare:112 | ||||
| chr19:48170266-48170699 | Common:2; Rare:118 | ||||
| chr19:48445901-48446046 | Common:1; Rare:58 | ||||
| chr19:48469050-48469390 | Common:3; Rare:97 | ||||
| chr19:48619139-48619435 | Rare:96 | ||||
| chr19:48624060-48624381 | Common:1; Rare:76 | ||||
| chr19:48811010-48811129 | Rare:42 | ||||
| chr19:48835838-48835958 | Common:1; Rare:31 | ||||
| chr19:48918723-48919080 | Common:3; Rare:120 | ||||
| chr19:48965240-48965609 | Rare:115; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):7 | ||||
| chr19:48993266-48993576 | Common:3; Rare:137; Clinvar:3; Clinvar (benign):2 | ||||
| chr19:49085152-49085492 | Common:3; Rare:139 | ||||
| chr19:49114264-49114416 | Common:1; Rare:40 | ||||
| chr19:49157660-49157800 | Rare:40; Clinvar:1 | ||||
| chr19:49335301-49335452 | Rare:26 |